Rotavirus NSP4 is secreted from infected cells as an oligomeric lipoprotein and binds to glycosaminoglycans on the surface of non-infected cells

Virology Journal

Volumn 8, Issue , 2011, Pages

  Didsbury, Alicia ^a,b   Wang, Carol ^a,b   Verdon, Daniel ^a,b   Sewell, Mary A ^a,b   McIntosh, Julie D ^a,b   Taylor, John A ^b  

^a UNIVERSITY OF AUCKLAND   (New Zealand)

^b UNIVERSITY OF AUCKLAND   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPROTEIN; GLYCOSAMINOGLYCAN; LIPOPROTEIN; OLIGOMER; PHOSPHOLIPID; ROTAVIRUS NONSTRUCTURAL PROTEIN 4; NS28 PROTEIN, ROTAVIRUS; TOXIN; VIRUS PROTEIN;

ARTICLE; CELL LINE; CELL MEMBRANE; CELL SURFACE; HUMAN; HUMAN CELL; ION EXCHANGE CHROMATOGRAPHY; NONHUMAN; PROTEIN BINDING; PROTEIN SECRETION; ANIMAL; CELL STRAIN CACO 2; CELL STRAIN HT29; CHEMISTRY; COLON; CULTURE MEDIUM; CYTOLOGY; EPITHELIUM CELL; ISOLATION AND PURIFICATION; METABOLISM; PATHOGENICITY; PROTEIN MULTIMERIZATION; ROTAVIRUS; SECRETION; VIROLOGY;

ROTAVIRUS;

ANIMALS; CACO-2 CELLS; CELL MEMBRANE; COLON; CULTURE MEDIA, CONDITIONED; EPITHELIAL CELLS; GLYCOPROTEINS; GLYCOSAMINOGLYCANS; HT29 CELLS; HUMANS; LIPOPROTEINS; PROTEIN MULTIMERIZATION; ROTAVIRUS; TOXINS, BIOLOGICAL; VIRAL NONSTRUCTURAL PROTEINS;

EID: 83655181346     PISSN: None     EISSN: 1743422X     Source Type: Journal    
DOI: 10.1186/1743-422X-8-551     Document Type: Article

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